核糖体晶体结构的研究历程——2009年度诺贝尔化学奖成果介绍

2009年度诺贝尔化学奖授予了美国科学家Venkatraman Ramakrishnan、Thomas A. Steitz和以色列科学家Ada E. Yonath,以表彰他们＂对核糖体结构和功能的研究＂。高分辨率的核糖体晶体结构使得人们能够在原子水平深入精确地理解核糖体的分子机制,并且为基于结构的合理化抗生素设计打下了坚实基础。以色列女科学家Ada E. Yonath是整个核糖体晶体结构研究领域的核心人物,她10多年坚持不懈地进行多种细菌核糖体的提纯与晶体生长工作,才使得核糖体高分辨率晶体结构解析成为可能。本文对2009年度诺贝尔化学奖的研究工作进行简要介绍。     

Strained silicon as a new electro-optic material

For decades, silicon has been the material of choice for mass fabrication of electronics. This is in contrast to photonics, where passive optical components in silicon have only recently been realized. The slow progress within silicon optoelectronics, where electronic and optical functionalities can be integrated into monolithic components based on the versatile silicon platform, is due to the limited active optical properties of silicon. Recently, however, a continuous-wave Raman silicon laser was demonstrated; if an effective modulator could also be realized in silicon, data processing and transmission could potentially be performed by all-silicon electronic and optical components. Here we have discovered that a significant linear electro-optic effect is induced in silicon by breaking the crystal symmetry. The symmetry is broken by depositing a straining layer on top of a silicon waveguide, and the induced nonlinear coefficient, chi(2) approximately 15 pm V(-1), makes it possible to realize a silicon electro-optic modulator. The strain-induced linear electro-optic effect may be used to remove a bottleneck in modern computers by replacing the electronic bus with a much faster optical alternative.     

Uptake of bacterial H3-DNA into fish embryos

Zusammenfassung H³-DNA vonSalmonella typhimurium wurde in den Dotter vonPlatypoecilus maculatus-Embryonen injiziert und ihr Verbleib untersucht. Nach 45 Stunden findet man 45% der injizierten H³-DNA-Radioaktivität in der säurelöslichen Fraktion des Dotters. Von diesem Zeitpunkt an nimmt die Radioaktivität in der säureunlöslichen Fraktion der Embryonen ständig zu, bis nach 140 Stunden ein Wert von 50% erreicht ist. Der hohe Anteil an radioaktivem säurenunlöslichem Material im Dotter, der 140 Stunden nach der Injektion noch ca. 35% beträgt, lässt vermuten, dass hier noch hochmolekulare Bakterien-DNA vorhanden ist. Somit erscheint die Möglichkeit einer Aufnahme dieser hochmolekularen DNA in die Embryozellen nicht ausgeschlossen.     

Sortilin is essential for proNGF-induced neuronal cell death

Sortilin (approximately 95 kDa) is a member of the recently discovered family of Vps10p-domain receptors, and is expressed in a variety of tissues, notably brain, spinal cord and muscle. It acts as a receptor for neurotensin, but predominates in regions of the nervous system that neither synthesize nor respond to this neuropeptide, suggesting that sortilin has additional roles. Sortilin is expressed during embryogenesis in areas where nerve growth factor (NGF) and its precursor, proNGF, have well-characterized effects. These neurotrophins can be released by neuronal tissues, and they regulate neuronal development through cell survival and cell death signalling. NGF regulates cell survival and cell death via binding to two different receptors, TrkA and p75NTR (ref. 10). In contrast, proNGF selectively induces apoptosis through p75NTR but not TrkA. However, not all p75NTR-expressing cells respond to proNGF, suggesting that additional membrane proteins are required for the induction of cell death. Here we report that proNGF creates a signalling complex by simultaneously binding to p75NTR and sortilin. Thus sortilin acts as a co-receptor and molecular switch governing the p75NTR-mediated pro-apoptotic signal induced by proNGF.     

Zircon U-Pb SHRIMP dating of the Yematan batholith in Dulan,North Qaidam,NW China

The Yematan batholith crops out over 120 km^2 in the North Qaidam ultrahigh pressure (UHP) metamorphic belt. It consists of granodiorite, monzogranite and biotite granite and forms an irregular intrusion into Neoproterozoic gneiss that has undergone Caledonian UHP metamorphism. Zircons from the Yematan granodiorite yield a SHRIMP U-Pb age of 397 3 Ma. These granitic rocks have geochemical characteristics intermediate between I- and S-type granites, and are post-collisional. We suggest that the Yematan granitic rocks were formed during the last exhumation event of the North Qaidam UHP belt.     

Young chondrules in CB chondrites from a giant impact in the early Solar System

Chondrules, which are the major constituent of chondritic meteorites, are believed to have formed during brief, localized, repetitive melting of dust (probably caused by shock waves) in the protoplanetary disk around the early Sun. The ages of primitive chondrules in chondritic meteorites indicate that their formation started shortly after that of the calcium-aluminium-rich inclusions (4,567.2 +/- 0.7 Myr ago) and lasted for about 3 Myr, which is consistent with the dissipation timescale for protoplanetary disks around young solar-mass stars. Here we report the 207Pb-206Pb ages of chondrules in the metal-rich CB (Bencubbin-like) carbonaceous chondrites Gujba (4,562.7 +/- 0.5 Myr) and Hammadah al Hamra 237 (4,562.8 +/- 0.9 Myr), which formed during a single-stage, highly energetic event. Both the relatively young ages and the single-stage formation of the CB chondrules are inconsistent with formation during a nebular shock wave. We conclude that chondrules and metal grains in the CB chondrites formed from a vapour-melt plume produced by a giant impact between planetary embryos after dust in the protoplanetary disk had largely dissipated. These findings therefore provide evidence for planet-sized objects in the earliest asteroid belt, as required by current numerical simulations of planet formation in the inner Solar System.     

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

Antigen presentation to T cells by MHC molecules is essential for adaptive immune responses. To determine the exact position of a gene affecting expression of MHC molecules, we finely mapped a previously defined rat quantitative trait locus regulating MHC class II on microglia in an advanced intercross line. We identified a small interval including the gene MHC class II transactivator (Mhc2ta) and, using a map over six inbred strains combined with gene sequencing and expression analysis, two conserved Mhc2ta haplotypes segregating with MHC class II levels. In humans, a -168A --> G polymorphism in the type III promoter of the MHC class II transactivator (MHC2TA) was associated with increased susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction, as well as lower expression of MHC2TA after stimulation of leukocytes with interferon-gamma. We conclude that polymorphisms in Mhc2ta and MHC2TA result in differential MHC molecule expression and are associated with susceptibility to common complex diseases with inflammatory components.     

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

We have previously reported a large Danish pedigree with autosomal dominant frontotemporal dementia (FTD) linked to chromosome 3 (FTD3). Here we identify a mutation in CHMP2B, encoding a component of the endosomal ESCRTIII complex, and show that it results in aberrant mRNA splicing in tissue samples from affected members of this family. We also describe an additional missense mutation in an unrelated individual with FTD. Aberration in the endosomal ESCRTIII complex may result in FTD and neurodegenerative disease.